Cedent Consulting Inc
Senior Research Associate (Global Drug Product Development and Manufacturing) (B
Cedent Consulting Inc, Boston, Massachusetts, us, 02298
Senior Research Associate (Global Drug Product Development and Manufacturing) (Boston, MA)
Senior Research Associate (SRA) - Global Drug Product Development and ManufacturingResponsibilities:Execute formulation, process development, and stability studies for both liquid and lyophilized products throughout the development lifecycle, from early-phase (Phase 1) through late-phase (Phase 3).Analyze, compile, and present data to support decision-making for drug product development programs.Participate in laboratory management and safety programs, including the implementation of new equipment and work processes.Maintain accurate and detailed documentation, including electronic lab notebook entries, and author comprehensive technical reports.Support the development and implementation of technological applications, such as iLab and other relevant systems.Requirements:Master’s degree in biology, molecular biology, chemistry, biochemistry, pharmaceutical sciences, chemical or protein engineering, or a related field; OR a bachelor’s degree with 2 years of relevant experience.Experience with analytical and biophysical characterization techniques such as HPLC, HIAC, MFI, CE-SDS, cIEF, and spectroscopy methods.Basic understanding of statistical data analysis.Ability to work in a team and project-oriented environment, with strong motivation, work ethic, and good communication skills.Flexible mindset to thrive in a fast-paced team setting.Preferred Qualifications:Previous experience in process or lyophilization development.
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Senior Research Associate (SRA) - Global Drug Product Development and ManufacturingResponsibilities:Execute formulation, process development, and stability studies for both liquid and lyophilized products throughout the development lifecycle, from early-phase (Phase 1) through late-phase (Phase 3).Analyze, compile, and present data to support decision-making for drug product development programs.Participate in laboratory management and safety programs, including the implementation of new equipment and work processes.Maintain accurate and detailed documentation, including electronic lab notebook entries, and author comprehensive technical reports.Support the development and implementation of technological applications, such as iLab and other relevant systems.Requirements:Master’s degree in biology, molecular biology, chemistry, biochemistry, pharmaceutical sciences, chemical or protein engineering, or a related field; OR a bachelor’s degree with 2 years of relevant experience.Experience with analytical and biophysical characterization techniques such as HPLC, HIAC, MFI, CE-SDS, cIEF, and spectroscopy methods.Basic understanding of statistical data analysis.Ability to work in a team and project-oriented environment, with strong motivation, work ethic, and good communication skills.Flexible mindset to thrive in a fast-paced team setting.Preferred Qualifications:Previous experience in process or lyophilization development.
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